Department of Physiology and Pharmacology, University of Bristol, Bristol, BS8 1TD, UK.
J Cell Sci. 2009 Nov 15;122(Pt 22):4186-94. doi: 10.1242/jcs.058420. Epub 2009 Oct 27.
Trafficking motifs present in the intracellular regions of ion channels affect their subcellular location within neurons. The mechanisms that control trafficking to dendrites of central neurons have been identified, but it is not fully understood how channels are localized to the soma. We have now identified a motif within the calcium-activated potassium channel K(Ca)2.1 (SK1) that results in somatic localization. Transfection of hippocampal neurons with K(Ca)2.1 subunits causes expression of functional channels in only the soma and proximal processes. By contrast, expressed K(Ca)2.3 subunits are located throughout the processes of transfected neurons. Point mutation of K(Ca)2.1 within this novel motif to mimic a sequence present in the C-terminus of K(Ca)2.3 causes expression of K(Ca)2.1 subunits throughout the processes. We also demonstrate that blocking of clathrin-mediated endocytosis causes K(Ca)2.1 subunit expression to mimic that of the mutated subunit. The role of this novel motif is therefore not to directly target trafficking of the channel to subcellular compartments, but to regulate channel location by subjecting it to rapid clathrin-mediated endocytosis.
在离子通道细胞内区域存在的运输基序会影响其在神经元内的亚细胞定位。已经确定了控制中枢神经元树突运输的机制,但通道如何定位于神经元体还不完全清楚。我们现在已经在钙激活钾通道 K(Ca)2.1(SK1)中鉴定出一个导致体细胞定位的基序。用 K(Ca)2.1 亚基转染海马神经元只会导致功能性通道在神经元体和近端突起中表达。相比之下,表达的 K(Ca)2.3 亚基分布在转染神经元的整个突起中。该新型基序中 K(Ca)2.1 的点突变模拟了 K(Ca)2.3 末端的序列,导致 K(Ca)2.1 亚基在整个突起中表达。我们还证明,网格蛋白介导的内吞作用的阻断会导致 K(Ca)2.1 亚基的表达模拟突变亚基的表达。因此,这个新型基序的作用不是直接将通道靶向运输到亚细胞隔室,而是通过使其快速发生网格蛋白介导的内吞作用来调节通道位置。